FDA.reportPublic FDA data

Morphe gel hand sanitizer

Manufacturer
BBC GROUP LIMITED
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:21:36

Label at a glance#

ProductMorphe gel hand sanitizer 01
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient .............purpose

alcohol Denat.: 75%(v/v)..... Antiseptic

Use

INDICATIONS & USAGE SECTION

Use for hand-washing to decrease bacteria on the skin, only when water is not available.

Warnings

WARNINGS SECTION

For external use only-hands

Flammable, keep away from fire and flames.

When using this product

OTC - WHEN USING SECTION

- do not get into eyes.

-if contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

-irritation and redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 8 use under adult supervision

Direction

DOSAGE & ADMINISTRATION SECTION

-Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Denatonium Benzoate, Tocopheryl Acetate （Vitamin E）

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76383-091-0176383-091-01

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76383-09176383-091-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
CUCUMBERYY7C30VXJTIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
ALCOHOL3K9958V90MACTIB
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
aa87863d-ba85-f55e-e053-2995a90aa3b0a9d6bc2d-9929-55df-e053-2995a90abaa02020-07-16WarningsExact identifier
spl set id: a9d6bc2d-9929-55df-e053-2995a90abaa0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.